Thiothixene Hcl
Drug - Thiothixene Hcl
The trade name of the product as shown on the labeling.
Dosage -
CONCENTRATE; ORAL
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Thiothixene Hydrochloride
Multiple ingredients are in alphabetical order.
Strength -
EQ 1MG BASE/ML
The potency of the active ingredient(s), Thiothixene Hydrochloride. May repeat for multiple part products.
Applicant -
PACO
The firm name holding legal responsibility for Thiothixene Hcl. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
071917
The FDA assigned number to Thiothixene Hcl. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Thiothixene Hcl. Each strength is a separate product. May repeat for multiple part products. Format is nnn.
Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.
Approval Date -
Sep 20, 1989
The date Thiothixene Hcl was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".
Reference Listed Drug (RLD) -
No
The pioneer or innovator of Thiothixene Hcl. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
Type -
DISCN
The group or category of approved drugs Thiothixene Hcl is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Paco Research Corp
The full name of the firm holding legal responsibility for the new application of Thiothixene Hcl.
Thiothixene Hcl
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